fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices training seminars workshops and conferences in AA

findaseminar logo balls FindaSeminar.com
event search registration and marketing services since 2002
Advanced Search
 
 

 

Public Seminar Training (33) On Site Training (26)

 

   
 

 

 

Your search for 'fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices' training seminars workshops and conferences in US and Canada has produced the following results.

 Applying Human Factors and Usability Engineering Throughout the Medical Device Development Lifecycle

 

Category: MEDICINE/NURSING

Training Provider: Online Compliance Panel

This session will describe techniques that, when applied appropriately, can greatly impact product safety and usability.

      
 

 Current Regulatory and Compliance Trends in the Area of Consent Decree in Pharmaceutical, Medical Device and Biologics Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar will discuss trends In Consent Decree, Current Food and Drug Administration trends, regulatory trends focusing on Computer Systems Validation, more.

      
 

 Design Reviews and Design Controls to meet FDA Requirements Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Attend this webinar to learn the objectives of having design controls in medical device manufacturing, and elements of design controls.

      
 

 Due Diligence of Quality Systems for Medical Device Companies Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Webinar on Due Diligence of Quality Systems for Medical Device Companies. Poor due diligence can lead to issues like recalls or warning letters.

      
 

 Effective Purchasing and Supplier Controls for Medical Device Manufacturers Webinar

 

Category:

Training Provider: Online Compliance Panel

This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products to your customers. Learn how to prevent quality and compliance problems by having a strong system for Purchasing Controls! This webinar will help you to understand the regulations and how you can translate them into an efficient and effective process for purchasing/ supplier control.

      
 

 FDA Regulations for Importing and Exporting Medical Devices Webinar

 

Category: MEDICINE/NURSING

Training Provider: Online Compliance Panel

Attend this webinar to understand how to better manage your import and export compliance activities and help support your logistics supply chain.

      
 

 FDA's New Endotoxin Test Guidance for Human Parenteral Drugs, Biological Products and Medical Devices Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Learn current testing requirements, what happened to the old LAL Guidance for industry document, documents supporting this new Guidance, more.

      
 

 Key Considerations in Verification & Validation of Medical Devices Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar will cite what are the key considerations in medical device design and validation that can help prevent FDA 483s.

      
 

 Medical Device - Engineering Change Control Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar can help you control your engineering change process, reduce your change order cycle times and eliminate ambiguity when communicating product changes to your extended supply chain.

      
 

 Medical Device Reporting (MDR) - By Compliance Global Inc.

 

Category: Compliance-Regulation

Training Provider: Compliance Global

webinar on Medical Device Reporting for The FDA expects health care professionals, patients, caregivers and consumers to submit voluntary reports about serious adverse events

      
 

 Medical Device Reporting Requirements for Manufacturers Final Guidance

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar explains the MDR regulation considering the new information contained in the Guidance and describes a compliant MDR procedure. Areas covered will include death, injury and mal-function reporting requirements, record keeping requirements, report timing, clarification of the term ‘becoming aware’ and clarification of reporting using electronic form 3500A.

      
 

 Medical Devices in the EU: CE Mark and Medical Device Directive 93/42/EEC Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Learn about requirements to apply for CE mark and meeting compliance expectations, changes to the EU Medical Devices Directive.

      
 

 Mobile Medical Apps (Is It a FDA Regulated Device?) and Cybersecurity

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

With mobile platforms more user friendly, and with computers, tablets and smart phones becoming more powerful, we see an increase in the offering of apps. Some of these apps are specifically targeted to assist individuals in the management of their health and wellness, while other apps are targeted to healthcare providers as tools to assist in the delivery of care.

      
 

 New ISO Standard for Medical Device Quality Systems 13485: 2016 Summary of its Impact to the Medical Device Industry Professionals Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

You will gain a thorough insight into the specific quality system requirements of all new International ISO 13485:2016 Quality System Standard requirements for Medical Devices. This timely and extremely informative webinar will truly build your knowledge from the fundamental quality principles. It will help you grow into fulfilling the quality and regulatory requirements as a professional working for medical device manufacturers of fully assembled devices and global suppliers manufacturing critical parts for the medical device industry. All noteworthy changes implemented into this key international standard will be discussed to pave the path for implementation of the changes in your organization.

      
 

 Path paved by the International Standard for ISO 9001:2015 for ISO 13485, the Medical Device Standard Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar details on ISO 13485, areas of emphasis, its correlation to the FDA 21 CFR 820 for medical device Quality System Management

      
 

 Preparing a US FDA Medical Device 510(k) Submission and Deciding When to Submit a 510(k) for a Change to an Existing Device Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar ensures your company gets a broader perspective of how and what to do to get a quick and non-debatable or questionable approval for your 510K product. All are different so this presentation will not just be specific for a specified Medical Device that is currently being marketed and your company wants the same opportunity to produce and sell that product.

      
 

 Security Essentials For Employees-Technology-Based Security Webinar

 

Category: GENERAL MGMT

Training Provider: National Seminars Training Group

This training sheds light on how to make yourself less vulnerable, how to protect your identity, your business, your customers.

      
 

 Software Verification and Validation in Medical Industry - By Compliance Global Inc.

 

Category: Compliance-Regulation

Training Provider: Compliance Global

Webinar On Validation in Medical Industry for The verification and validation of medical software is coming under increased scrutiny by the U.S. FDA

      
 

 Special Considerations during Medical Device Design: Dos and Don'ts Webinar

 

Category: MEDICINE/NURSING

Training Provider: Online Compliance Panel

In the past, the designer was in charge of everything that could go wrong in the product performance. Today product's manufacturing processes, supply chain controls, and product users have become disengaged in many companies: therefore most design engineers are far removed from many things going wrong.

      
 

 Strategies for 510 (k) Applications for Medical Devices Software Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

Several medical devices use either off-the-shelf or custom software. A couple of guidance documents from FDA written almost a decade ago are the only official comments from FDA to assist manufacturers understand the current FDA requirements.

      
 

 Test Method Validation to Verify your Device Performance Webinar

 

Category: Compliance-Regulation

Training Provider: Online Compliance Panel

This webinar will help you have an understanding of Test Method Validations to verify the performance of a Medical Device, global reference standards, the FDA requirements and how to perform successful TMV to ensure your inspection of verification is effective, using detailed real-life case studies.

      
 

 Understanding the Brazilian Regulatory Environment for Medical Devices

 

Category: MEDICINE/NURSING

Training Provider: Online Compliance Panel

The Brazilian Health Surveillance Agency (ANVISA) was created in 1999 and it is the Entity responsible for regulating medical devices marketed in Brazil. ANVISA is also in charge for post-market surveillance. Brazil is the largest market for medical devices in South America and presents a significant challenge for regulators looking to navigate its complex and dynamic regulatory system. This webinar showcases the regulatory environment and the recent updates from ANVISA in Brazil.

      
 

Didn't find the training you want?
Start a new keyword search
search all seminars in US and Canada

SEMINAR MARKETING SERVICES

Reach training seekers with specific interest in fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices training seminars, online fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices training, and fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices training products and services.
Add your Training Seminars, Online Training events and products, and Onsite Training services and start reaching highly qualified training seekers today!

Search Instructions

Click the button to view
upcoming dates & locations 
for fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices training seminars.
Then click
to view the event details and register for the fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices seminar date and location of your choice.

Narrow your search Find fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices seminars by State & City ... click here

Send these search results to your manager or HR Rep

Your email:

Recipient's email:

 

view search results by state

Click any state below to find upcoming fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices training seminars that match your training search query.

United States

All States
Alabama
Alaska
Arizona
Arkansas
California
Colorado
Connecticut
D.C.
Delaware
Florida
Georgia
Hawaii
Idaho
Illinois
Indiana
Iowa
Kansas
Kentucky
Louisiana
Maine
Maryland
Massachusetts
Michigan
Minnesota
Mississippi
Missouri
Montana
Nebraska
Nevada
New Hampshire
New Jersey
New Mexico
New York
North Carolina
North Dakota
Ohio
Oklahoma
Oregon
Pennsylvania
Rhode Island
South Carolina
South Dakota
Tennessee
Texas
Utah
Vermont
Virginia
Washington
West Virginia
Wisconsin
Wyoming

Canada

Alberta
British Columbia
Saskatchewan
Manitoba
Ontario
Quebec
New Brunswick
Nova Scotia
Prince Edward Island
Newfoundland

Puerto Rico

Puerto Rico

About this seminar search engine:

FindaSeminar.com is the quickest way to find and register for fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices training seminars in your local city and around the U.S. and Canada.  We are constantly adding new dates and locations for thousands of the most popular seminars and training events offered.

Bookmark FindaSeminar and visit often to find upcoming fda federal drugs administration endotoxin testing tests human parenteral biological products medical devices training seminars workshops and conferences in the U.S. and Canada. 

FREE Training Offer        
Claim your free Customer Service training guide and or  free Time Management training guide now!